Description

Jointly Accurate Sv Merging with Intersample Network Edges

Input

name:type
description
pattern

meta:map

Groovy Map containing sample information e.g. [ id:‘test’, single_end:false ]

vcfs:list

The VCF files that need to be merged

*.{vcf,vcf.gz}

bams:list

Optional - The BAM files from which the VCFs were created

*.bam

sample_dists:file

Optional - A txt file containing the distance thresholds for each sample

*.txt

meta2:map

Groovy Map containing fasta information e.g. [ id:‘test’, single_end:false ]

fasta:file

Optional - The reference FASTA file used to create the VCFs

*.{fasta,fa}

meta3:map

Groovy Map containing fasta index information e.g. [ id:‘test’, single_end:false ]

fasta_fai:file

Optional - The index of the reference FASTA file used to create the VCFs

*.fai

chr_norm:file

Optional - A txt file containing the chromosomes and their aliases for normalization

*.txt

Output

name:type
description
pattern

vcf

meta:map

Groovy Map containing sample information e.g. [ id:‘test’, single_end:false ]

*.vcf.gz:file

The merged VCF file

*.vcf.gz

versions

versions.yml:file

File containing software versions

versions.yml

Tools

jasminesv
MIT

Software for merging structural variants between individuals